Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Mafenide Hydrochloride | HCID 67313 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | Ethylthiourea | HCID 3032338 | — |
| Edukt | 1,3-Bisbenzoyl-1-ethyl-2-methylisothiourea | HCID 22154506 | — |
| Edukt | HCID 178464634 | HCID 178464634 | — |
| Edukt | HCID 178514169 | HCID 178514169 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | HCID 178464747 | HCID 178464747 | — |
Reaktionsschritte
To 36 g. of 1-ethylthiourea in 200 ml. of acetone was added 70 g. of methyliodide. Evaporation of the solvent gave 71 g. of 1-ethyl-2-methylisothiourea hydroiodide as colorless crystals, m.p. 84°-87° C. This isothiurea, 23.2 g., was reacted with a total of 30 ml. of benzoyl chloride and after 6 hours the solution was poured onto ice. The mixture was made basic with NaOH and the crystals which formed were collected by filtration to give 27.8 g. of 1,3-bisbenzoyl-1-ethyl-2-methylisothiourea, m.p. 84°-86° C. This bisbenzoylisothiourea, 3.1 g., was reacted with 2.4 g. of 4-aminomethylbenzenesulfonamide hydrochloride and 1.5 g. of sodium acetate in 250 ml. of isopropyl alcohol. Aqueous work-up followed by dichloromathane extraction and evaporation gave the title compound as a colorless glass, m.p. 70°-80° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04977189 |
|---|
| Quelldatensatz | uspto-grants-1990_12 |
|---|
| ORD ID | ord-e672424bc46e4ba99cfb0f8c6788beb2 |
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| Quellennotiz | uspto-grants-1990_12 |
|---|